VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome

The loss of a single copy of TBX1 accounts for most of the clinical signs and symptoms of 22q11.2 deletion syndrome, a common genetic disorder that is characterized by multiple congenital anomalies and brain-related clinical problems, some of which likely have vascular origins. Tbx1 mutant mice have...

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Detalles Bibliográficos
Autores principales: Cioffi, Sara, Flore, Gemma, Martucciello, Stefania, Bilio, Marchesa, Turturo, Maria Giuseppina, Illingworth, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553901/
https://www.ncbi.nlm.nih.gov/pubmed/36216515
http://dx.doi.org/10.26508/lsa.202101308

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